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Siderosis - 40 Studies Found
Estado | Estudiar |
Withdrawn |
Nombre del estudio: Treatment of Iron Overload Requiring Chelation Therapy Condición:
|
Enrolling by invitation |
Nombre del estudio: A Case Control Study to Evaluate the Cognitive and Brain Function of β-thalassemia Patients. Condición:
Fecha: 2013-08-07 |
Enrolling by invitation |
Nombre del estudio: PHOX2B Mutation-Confirmed Congenital Central Hypoventilation Syndrome in A Chinese Family: Presentations From Newborn to Adulthood Condición: Central Alveolar Hypoventilation Syndrome Fecha: 2008-04-01 Intervenciones: Device: CPAP CPAP treatment for patients with congenital central hypoventilation syndrome |
Completed |
Nombre del estudio: Evaluation of the Safety, Tolerability, Pharmacokinetics (PK) and Effects on Liver Iron Concentration of ICL670 Relative to Deferoxamine(DFO). Condición: Sickle Cell Disease Fecha: 2010-03-15 Intervenciones: Drug: ICL670 Daily doses of ICL670 were taken orally 30 minutes before breakfast. The doses range from 5 |
Completed |
Nombre del estudio: A Protocol to Allow Treatment With ICL670 for Patients With or at Risk of Life-threatening Complications of Transfusional Iron Overload Who Are Unable to Tolerate Other Iron Chelators Because of Documented Severe Toxicity Condición: Transfusional Iron Overload Fecha: 2010-01-05 Intervenciones: Drug: ICL670 |
Not yet recruiting |
Nombre del estudio: Efficacy of Bone Marrow Mesenchymal Stem Cell in Pulmonary Hemosiderosis Condición: Idiopathic Pulmonary Hemosiderosis Fecha: 2016-12-03 Intervenciones: Biological: Bone marrow mesenchymal stem cells in treatment of Idiopathic pulmonary hemosiderosis |
Not yet recruiting |
Nombre del estudio: PHOX2B Mutation-Confirmed Congenital Central Hypoventilation Syndrome in A Chinese Family: Presentations From Newborn to Adulthood Condición: Central Alveolar Hypoventilation Syndrome Fecha: 2008-04-01 Intervenciones: Device: CPAP CPAP treatment for patients with congenital central hypoventilation syndrome |
Active, not recruiting |
Nombre del estudio: Observational Study of Deferiprone (Ferriprox®) in the Treatment of Superficial Siderosis Condición: Superficial Siderosis Fecha: 2011-01-20 |
Completed |
Nombre del estudio: A Prospective Safety Follow Up Study Of Subjects Enrolled In Study A4321001 And Who Have Received Drug Product Condición: Siderosis Fecha: 2007-05-07 Intervenciones: Other: Observational Trial No intervention is being used in this study. |
Completed |
Nombre del estudio: An Epidemiological Study to Assess Iron Overload Using MRI in Patients With Transfusional Siderosis (TIMES Study) Condición: Thalassemia, Non-transfusional-dependent Thalassemia (NTDT), Myeloplastic Dysplasia (MDS), Other Anemia Fecha: 2012-11-26 Intervenciones: Device: MRI scan MRI was used to measure both liver and cardiac iron loading (R2 by FerriScan and T2*, r |